Linked Data
dbSNP Id:
rs1882902603
gnomAD v3:
14-21324934-C-T
gnomAD v4:
14-21324934-C-T
MyVariant Identifiers:
chr14:g.21793093C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.21324934C>T , CM000676.2:g.21324934C>T | GRCh38 |
| NC_000014.8:g.21793093C>T , CM000676.1:g.21793093C>T | GRCh37 |
| NC_000014.7:g.20862933C>T | NCBI36 |
| NG_008933.1:g.41958C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000400017.7:c.2079C>T MANE Select | ENSP00000382895.2:p.Tyr693= | |
| ENST00000382933.8:c.689-2689C>T | ENSP00000372391.4:n.689-2689C>T | |
| ENST00000400017.6:c.2079C>T | ENSP00000382895.2:p.Tyr693= | |
| ENST00000553500.5:n.328+209C>T | ||
| ENST00000553927.1:n.1011C>T | ||
| ENST00000555322.5:c.506C>T | ||
| ENST00000555489.5:c.272C>T | ENSP00000451044.1:n.272C>T | |
| ENST00000555587.5:c.504C>T | ENSP00000451262.1:p.Tyr168= | |
| ENST00000556336.5:c.1682-2689C>T | ENSP00000450445.1:n.1682-2689C>T | |
| ENST00000557771.5:c.1965C>T | ENSP00000451219.1:p.Tyr655= | |
| NM_020366.3:c.2079C>T | NP_065099.3:p.Tyr693= | |
| XM_005267879.2:c.1005C>T | XP_005267936.1:p.Tyr335= | |
| XM_005267880.2:c.972C>T | XP_005267937.1:p.Tyr324= | |
| XM_005267881.2:c.453C>T | XP_005267938.1:p.Tyr151= | |
| XM_011536978.1:c.1005C>T | XP_011535280.1:p.Tyr335= | |
| XM_011536979.1:c.797-8C>T | XP_011535281.1:n.797-8C>T | |
| XM_011536980.1:c.796+209C>T | XP_011535282.1:n.796+209C>T | |
| XM_011536981.1:c.1005C>T | XP_011535283.1:p.Tyr335= | |
| XM_011536982.1:c.796+209C>T | XP_011535284.1:n.796+209C>T | |
| XM_011536983.1:c.2046C>T | XP_011535285.1:p.Tyr682= | |
| XM_005267881.3:c.453C>T | XP_005267938.1:p.Tyr151= | |
| XM_017021473.1:c.1005C>T | XP_016876962.1:p.Tyr335= | |
| XM_024449663.1:c.1005C>T | XP_024305431.1:p.Tyr335= | |
| XM_024449664.1:c.1005C>T | XP_024305432.1:p.Tyr335= | |
| XM_024449665.1:c.796+209C>T | XP_024305433.1:n.796+209C>T | |
| XM_024449666.1:c.796+209C>T | XP_024305434.1:n.796+209C>T | |
| NM_001377523.1:c.689-2689C>T | NP_001364452.1:n.689-2689C>T | |
| NM_001377948.1:c.1005C>T | NP_001364877.1:p.Tyr335= | |
| NM_001377949.1:c.796+209C>T | NP_001364878.1:n.796+209C>T | |
| NM_001377950.1:c.689-2689C>T | NP_001364879.1:n.689-2689C>T | |
| NM_001377951.1:c.191-2689C>T | NP_001364880.1:n.191-2689C>T | |
| NM_020366.4:c.2079C>T MANE Select | NP_065099.3:p.Tyr693= |